STEMONIDINE Chemische Eigenschaften,Einsatz,Produktion Methoden
Beschreibung
This alkaloid occurs in the roots of Stemona japonica and behaves as a tertiary
base. It has [α]
25D - 7.65°C and is characterized as the hydrochloride which
decomposes at 2600 C and the methiodide, decomposing at 2480 C. The alkaloid is
not affected by HCI in either AcOH or EtOH and the oxidation products formed
with KMn04 depend upon the conditions. If the oxidation is carried out in
Me2CO a base is obtained which yields a crystalline methiodide, m.p. 235°C. On
the other hand, KMn04 in dilute H2 S04 at lOoC yields two substances (a) a
neutral compound, C16H230sN, m.p. 208°C; [α]
D - 58.30 which contains a
lactone ring and one methoxyl group and (b) a substance CllH170 4N, m.p.
202°C; [α]
D - 24.17° which yields a semicarbazone, m.p. 258°C but contains
no lactone group.
There is still ~ome doubt concerning the plant identity from which this alka_x0002_loid was isolated. Investigation by Suzuki suggested that it is not Stemona
japonica as stated above but Stemona ovata Nakai.
Einzelnachweise
Suzuki.,J. Pharm. Soc., Japan, No. 352, 567 (1921)
Suzuki., ibid, 49, 78,457 (1929)
Suzuki., ibid, 51,43 (1931)
Suzuki., ibid, 54, 101 (1934)
Suzuki., ibid, 59, 184(1939)
STEMONIDINE Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
